4.7 Article

Enhanced Performance of Carbon-Selenide Composite with La0.9Ce0.1NiO3 Perovskite Oxide for Outstanding Counter Electrodes in Platinum-Free Dye-Sensitized Solar Cells

Journal

NANOMATERIALS
Volume 12, Issue 6, Pages -

Publisher

MDPI
DOI: 10.3390/nano12060961

Keywords

counter electrode; perovskite oxide; carbon materials; metal selenides; metal-organic-frameworks

Funding

  1. National Natural Science Foundation of China [51972255]
  2. Scientific Leadership Training Program of Hubei Province
  3. Students' Innovation and Entrepreneurship Training Program [20171049701024]
  4. Chinese Scholarship Council (CSC) [2016GF147]
  5. Fundamental Research Funds for the Central Universities [GK202102001]

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This study demonstrates that the L@F@CB composite materials, synthesized by mixing La0.9Ce0.1NiO3 and functionalized multiwall carbon nanotubes, exhibit excellent electrocatalytic activity in dye-sensitized solar cells, making them potential alternatives to the traditional platinum-based counter electrode.
For large-scale applications, dye-sensitized solar cells (DSSCs) require the replacement of the scarce platinum (Pt)-based counter electrode (CE) with efficient and cheap alternatives. In this respect, low-cost perovskite oxides (ABO(3)) have been introduced as promising additives to composite-based CEs in Pt-free DSSCs. Herein, we synthesized composites from La0.9Ce0.1NiO3 (L) perovskite oxide and functionalized-multiwall-carbon-nanotubes wrapped in selenides derived from metal-organic-frameworks (f-MWCNT-ZnSe-CoSe2, F). L and F were then mixed with carbon black (CB) in different mass ratios to prepare L@CB, F@CB, and L@F@CB composites. The electrochemical analysis revealed that the L@F@CB composite with a mass ratio of 1.5:3:1.5 exhibits better electrocatalytic activity than Pt. In addition, the related DSSC reached a better PCE of 7.49% compared to its Pt-based counterpart (7.09%). This improved performance is the result of the increase in the oxygen vacancy by L due to the replacement of La with Ce in its structure, leading to more active sites in the L@F@CB composites. Moreover, the F@CB composite favors the contribution to the high electrical conductivity of the hybrid carbon nanotube-carbon black, which also offers good stability to the L@F@CB CE by not showing any obvious change in morphology and peak-to-peak separation even after 100 cyclic voltammetry cycles. Consequently, the corresponding L@F@CB-based device achieved enhanced stability. Our work demonstrates that L@F@CB composites with a low cost are excellent alternatives to Pt CE in DSSCs.

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